期刊
VACUUM
卷 210, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.vacuum.2023.111899
关键词
Bi4Ti3O12; Amphoteric photoelectrodes; Oxygen vacancies; Photoelectrochemistry
Bi4Ti3O12 (BTO) photoelectrodes were prepared using a sol-gel spin coating method, and the oxygen vacancy (OV) concentrations in BTO were regulated through heat-treatment in different atmospheres. The introduction of OVs in BTO after Ar processing resulted in an interesting p/n type amphoteric photo-response characteristic. The enhanced photoelectrochemical properties of Ar-BTO were attributed to the abundant OVs, which effectively inhibited recombination, boosted carrier injection efficiency, and activated the electrode surface.
Bi4Ti3O12 (BTO) photoelectrodes were fabricated by a sol-gel spin coating method and oxygen vacancy (OV) concentrations in BTO were regulated through a following heat-treatment in different atmospheres. Based on the results of XRD, XPS and HRTEM, OVs have been introduced in BTO after Ar processing. An interesting p/n type amphoteric photo-response characteristic was discovered in BTO as demonstrated by the LSV, CV plots and open-circuit photovoltage measurement. The typical amphoteric photo-response characteristic of BTO should be related to its special Fermi level structure and accordingly minor band bending in the interface between BTO and the electrolyte. The positive photocurrent density of Ar-BTO is 0.75 mu A/cm(2) at 0.5 V vs. Ag/AgCl, which is 4.4 times over that of BTO, and its photocurrent onset potential showed an obvious negative shift (similar to 0.1 V) in relative to BTO. The charge carrier densities of Ar-BTO was over 60% higher than that of BTO. The enhanced photoelectrochemical properties of Ar-BTO was ascribed to its abundant OVs which effectively inhibited recombination, boosted carrier injection efficiency and activated electrode surface as demonstrated by the EIS and PL characterizations. These findings provide new perspective for fabricating new type bismuth-based photoelectrodes and optimizing its photoelectrochemical performance.
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